Canonical Allele Identifier: PA2827881869
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Met168Val
CA2490366
NM_001354606.2:c.502A>G