Canonical Allele Identifier: PA332938
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136117
ClinVar RCV Id: RCV000123319 RCV001019149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Leu11Val
CA009216
NM_020630.6:c.31C>G