Canonical Allele Identifier: PA658829159
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071504.2:p.Glu262Asp
CA312908
NM_022172.3:c.786G>T
CA381501485
NM_022172.3:c.786G>C