Canonical Allele Identifier: PA312912
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Arg1036His
CA312911
NM_000920.4:c.3107G>A