Canonical Allele Identifier: PA2828622444
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362539.1:p.Gln224His
CA114416
NM_001375610.1:c.672G>C
CA348401830
NM_001375610.1:c.672G>T