Canonical Allele Identifier: PA2828622435
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362539.1:p.Arg218Trp
CA114410
NM_001375610.1:c.652C>T