Canonical Allele Identifier: PA2827882516
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2948847
ClinVar RCV Id: RCV003809621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Asp465Gly
CA353559902
NM_001354607.2:c.1394A>G