Canonical Allele Identifier: PA2827882170
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1208422
ClinVar Variation Id: 1687701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Gly499Arg
CA2490690
NM_001354606.2:c.1495G>A
CA2490691
NM_001354606.2:c.1495G>C