Canonical Allele Identifier: PA2829942206
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1800643
ClinVar RCV Id: RCV002461782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Trp856Ser
CA376556630
NM_020630.6:c.2567G>C