Canonical Allele Identifier: PA2826151579
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1719314
ClinVar RCV Id: RCV002302074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Ser460Asn
CA77003533
NM_001184967.2:c.1379G>A