Allele Registry

Canonical Allele Identifier: PA106774

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014959

RCV000021789

RCV000566125

RCV002272020

ClinVar Variation:

13934

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys620Trp	CA008105 NM_020975.6:c.1860C>G