Canonical Allele Identifier: PA658670771
Gene: CIITA HGNC NCBI

Linked Data

ClinVar Variation Id: 459198
ClinVar RCV Id: RCV000545058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000237.2:p.Gly174Arg
CA277736969
NM_000246.4:c.520G>A
CA394728206
NM_000246.4:c.520G>C