Canonical Allele Identifier: PA2825220513
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 1380399
ClinVar RCV Id: RCV001886353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Phe848Leu
CA381492736
NM_000920.4:c.2544C>G
CA381492737
NM_000920.4:c.2544C>A
CA381492742
NM_000920.4:c.2542T>C