Canonical Allele Identifier: PA2826151393
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 375216
ClinVar RCV Id: RCV000416308 RCV000416288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Arg266Gly
CA16044011
NM_001184967.2:c.796A>G