Canonical Allele Identifier: PA2825105728
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1319604
ClinVar RCV Id: RCV003237600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Thr389Ala
CA353559941
NM_000248.4:c.1165A>G