Canonical Allele Identifier: PA2827881701
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2922092
ClinVar RCV Id: RCV003785306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.His401Leu
CA353559359
NM_001354605.2:c.1202A>T