Canonical Allele Identifier: PA2826151380
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1718943
ClinVar RCV Id: RCV002301782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.His258Gln
CA353561660
NM_001184967.2:c.774C>A
CA353561661
NM_001184967.2:c.774C>G