Canonical Allele Identifier: PA2827881801
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Gly505Glu
CA2490692
NM_001354605.2:c.1514G>A