Canonical Allele Identifier: PA2827882533
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1196677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Val480Met
CA77003529
NM_001354607.2:c.1438G>A