Canonical Allele Identifier: PA913200172
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 618261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Arg830His
CA6131047
NM_001040716.2:c.2489G>A