Canonical Allele Identifier: PA149122
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13938
ClinVar RCV Id: RCV000014965 RCV000034774 RCV000082055 RCV000202663 RCV000162949 RCV000320112 RCV000238890 RCV000354936 RCV000411820 RCV000410308 RCV000736279 RCV001080524 RCV001269493 RCV001822995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg982Cys
CA009143
NM_020630.6:c.2944C>T