Canonical Allele Identifier: PA2827882236
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Met152Val
CA2490366
NM_001354607.2:c.454A>G