Canonical Allele Identifier: PA2827881950
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 373914
ClinVar RCV Id: RCV000415280
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Amino-acid Alleles

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