Canonical Allele Identifier: PA2828621902
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362537.1:p.Gln207His
CA114416
NM_001375608.1:c.621G>C
CA348401830
NM_001375608.1:c.621G>T