Canonical Allele Identifier: PA312922
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203921
ClinVar RCV Id: RCV000186127 RCV000632922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Arg263Gln
CA312921
NM_000920.4:c.788G>A