Canonical Allele Identifier: PA2826774401
Gene: TAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 836124
ClinVar RCV Id: RCV001037174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276972.1:p.Leu383Pro
CA363583019
NM_001290043.2:c.1148T>C