Canonical Allele Identifier: PA2825105705
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1313653
ClinVar RCV Id: RCV001764017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Val366Ile
CA353559800
NM_000248.4:c.1096G>A