Canonical Allele Identifier: PA2825221071
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 305617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Ala1114Val
CA6130812
NM_000920.4:c.3341C>T