Canonical Allele Identifier: PA2828822487
Gene: CIITA HGNC NCBI

Linked Data

ClinVar Variation Id: 662433
ClinVar RCV Id: RCV000820074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366260.1:p.Phe871Leu
CA7900485
NM_001379331.1:c.2611T>C
CA394734987
NM_001379331.1:c.2613C>A
CA394734989
NM_001379331.1:c.2613C>G