Canonical Allele Identifier: PA213408
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 135177
ClinVar RCV Id: RCV000121979 RCV000202914 RCV000410377 RCV000411486 RCV000462996 RCV000573705 RCV002492438 RCV003151746 RCV003460858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr754Met
CA008622
NM_020630.6:c.2261C>T