Canonical Allele Identifier: PA2828622171
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362538.1:p.Gln218His
CA114416
NM_001375609.1:c.654G>C
CA348401830
NM_001375609.1:c.654G>T