Canonical Allele Identifier: PA128280
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13909
ClinVar RCV Id: RCV000014925 RCV000014924 RCV000129490 RCV000182582 RCV000421191 RCV000432822 RCV000422622 RCV000425364 RCV000476408 RCV000438527 RCV003989285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Cys634Tyr
CA008348
NM_020630.6:c.1901G>A