Canonical Allele Identifier: PA2826151267
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494
ClinVar RCV Id: RCV000288018 RCV000347693 RCV001568741 RCV002520178 RCV003422332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Met117Val
CA2490366
NM_001184967.2:c.349A>G