Canonical Allele Identifier: PA2825105229
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_000237.2:p.Phe920Leu
CA7900485
NM_000246.4:c.2758T>C
CA394734987
NM_000246.4:c.2760C>A
CA394734989
NM_000246.4:c.2760C>G