Canonical Allele Identifier: PA916015261
Gene: CIITA HGNC NCBI

Linked Data

ClinVar Variation Id: 459197
ClinVar RCV Id: RCV000533575 RCV003915500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273331.1:p.Thr166Ser
CA7899786
NM_001286402.1:c.497C>G
CA394728158
NM_001286402.1:c.496A>T