Canonical Allele Identifier: PA2826151349
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_001171896.1:p.Tyr213Cys
CA16043400
NM_001184967.2:c.638A>G