Canonical Allele Identifier: PA916065382
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071504.2:p.Lys589Asn
CA312851
NM_022172.3:c.1767G>T
CA381495040
NM_022172.3:c.1767G>C