Canonical Allele Identifier: PA2829651042
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Met168Val
CA2490366
NM_006722.2:c.502A>G