Allele Registry

Canonical Allele Identifier: PA161958

Gene: RET HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000034779

RCV000121992

RCV000276548

RCV000333869

RCV000354891

RCV000367517

RCV000565970

RCV000755685

RCV001083006

RCV003492298

ClinVar Variation:

24880

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Val292Met	CA009374 NM_020975.6:c.874G>A