Allele Registry

Canonical Allele Identifier: PA2827881950

Gene: MITF HGNC NCBI

ClinVar RCV:

RCV000415280

ClinVar Variation:

373914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341535.1:p.Tyr264Cys	CA16043400 NM_001354606.2:c.791A>G