Canonical Allele Identifier: PA2827882512
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2947768
ClinVar RCV Id: RCV003804398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Ile461Thr
CA353559875
NM_001354607.2:c.1382T>C