Canonical Allele Identifier: PA2825105692
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1721237
ClinVar RCV Id: RCV002294918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Thr356Ile
CA353559741
NM_000248.4:c.1067C>T