Canonical Allele Identifier: PA312920
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Val206Leu
CA312918
NM_001040716.2:c.616G>T
CA381502042
NM_001040716.2:c.616G>C