Canonical Allele Identifier: PA2827882841
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1305242
ClinVar RCV Id: RCV001768449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Gly406Val
CA353559748
NM_001354608.2:c.1217G>T