Allele Registry

Canonical Allele Identifier: PA161932

Gene: RET HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

45384

ClinVar RCV:

RCV000030402

RCV000034766

RCV000121985

RCV000148768

RCV000163266

RCV000202649

RCV001082759

RCV001108849

RCV001108850

RCV001108851

ClinVar Variation:

36723

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Leu56Met	CA007702 NM_020975.6:c.166C>A