Canonical Allele Identifier: PA312919
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Val206Leu
CA312918
NM_000920.4:c.616G>T
CA381502042
NM_000920.4:c.616G>C