Canonical Allele Identifier: PA2828620374
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362531.1:p.Gln287His
CA114416
NM_001375602.1:c.861G>C
CA348401830
NM_001375602.1:c.861G>T