Canonical Allele Identifier: PA2580407433
Gene: TAP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061313.2:p.Gly107Ala
CA363586592
NM_018833.3:c.320G>C