Canonical Allele Identifier: PA2827881780
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2948847
ClinVar RCV Id: RCV003809621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Asp487Gly
CA353559902
NM_001354605.2:c.1460A>G