Canonical Allele Identifier: PA2827881293
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.Met169Val
CA2490366
NM_001354604.2:c.505A>G