Canonical Allele Identifier: PA2826151389
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14272
ClinVar RCV Id: RCV000015342 RCV000498643 RCV000826199 RCV001290155 RCV001785452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Arg266del
CA645372387
NM_001184967.2:c.796_798del