ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826774398
Gene: TAP2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000014727
RCV000455533
RCV001517538
RCV001824569
ClinVar Variation:
13724
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001276972.1:p.Val379Ile
CA123397
NM_001290043.2:c.1135G>A