Canonical Allele Identifier: PA2827882162
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Pro491Ala
CA353559954
NM_001354606.2:c.1471C>G