Canonical Allele Identifier: PA128177
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13913
ClinVar RCV Id: RCV000014932 RCV002513055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Cys611Trp
CA007954
NM_020630.6:c.1833C>G