Canonical Allele Identifier: PA2827881908
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346495
ClinVar RCV Id: RCV000283175 RCV000405002 RCV000977275 RCV002257652 RCV002520179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.His214Leu
CA2490409
NM_001354606.2:c.641A>T