Canonical Allele Identifier: PA312932
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203924
ClinVar RCV Id: RCV000186130 RCV000675135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Thr908Met
CA312930
NM_001040716.2:c.2723C>T