Canonical Allele Identifier: PA2827882171
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Gly499Glu
CA2490692
NM_001354606.2:c.1496G>A