Canonical Allele Identifier: PA312913
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Arg1036His
CA312911
NM_001040716.2:c.3107G>A