Allele Registry

Canonical Allele Identifier: PA2827881919

Gene: MITF HGNC NCBI

ClinVar RCV:

RCV001355463

RCV003771039

ClinVar Variation:

1049403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341535.1:p.Asp224Gly	CA2490437 NM_001354606.2:c.671A>G