Canonical Allele Identifier: PA312909
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Glu262Asp
CA312908
NM_000920.4:c.786G>T
CA381501485
NM_000920.4:c.786G>C