Canonical Allele Identifier: PA312853
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Lys589Asn
CA312851
NM_001040716.2:c.1767G>T
CA381495040
NM_001040716.2:c.1767G>C