Allele Registry

Canonical Allele Identifier: PA2828048287

Gene: RET HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000014973

RCV000021853

RCV000021854

RCV000354366

RCV000419916

RCV000425568

RCV000426266

RCV000436948

RCV000437130

RCV000479688

RCV000487450

RCV000561258

RCV000596480

RCV002453279

RCV003226171

ClinVar Variation:

13946

38613

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Val550Leu	CA008758 NM_001355216.1:c.1648G>C CA008766 NM_001355216.1:c.1648G>T CA3060586028 NM_001355216.1:c.1647_1648delinsTT