Canonical Allele Identifier: PA2828620950
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362533.1:p.Gln247His
CA114416
NM_001375604.1:c.741G>C
CA348401830
NM_001375604.1:c.741G>T