Canonical Allele Identifier: PA2826774272
Gene: TAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2417584
ClinVar RCV Id: RCV003115053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276972.1:p.Gly107Ala
CA363586592
NM_001290043.2:c.320G>C