Canonical Allele Identifier: PA2827881723
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Val426Ala
CA2490635
NM_001354605.2:c.1277T>C