Canonical Allele Identifier: PA2827881942
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2115672
ClinVar RCV Id: RCV003046580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Pro255Thr
CA77001734
NM_001354606.2:c.763C>A