Canonical Allele Identifier: PA2827882067
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2662014
ClinVar RCV Id: RCV003443509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Ala394Thr
CA77003517
NM_001354606.2:c.1180G>A