Canonical Allele Identifier: PA1139728166
Gene: TAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 836124
ClinVar RCV Id: RCV001037174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061313.2:p.Leu383Pro
CA363583019
NM_018833.3:c.1148T>C