Canonical Allele Identifier: PA114418
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Gln226His
CA114416
NM_000312.4:c.678G>C
CA348401830
NM_000312.4:c.678G>T