Canonical Allele Identifier: PA2827882827
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2122013
ClinVar RCV Id: RCV003043486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Thr393Ala
CA353559663
NM_001354608.2:c.1177A>G