Canonical Allele Identifier: PA111797
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 21222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Arg631Gln
CA341754
NM_000920.4:c.1892G>A