Canonical Allele Identifier: PA2827882146
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2944207
ClinVar RCV Id: RCV003805957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Leu478Pro
CA353559881
NM_001354606.2:c.1433T>C