Canonical Allele Identifier: PA2827882884
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Gly448Glu
CA2490692
NM_001354608.2:c.1343G>A