Canonical Allele Identifier: PA2828622768
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362540.1:p.Ala301Val
CA114391
NM_001375611.1:c.902C>T