Canonical Allele Identifier: PA2828621317
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 858029
ClinVar RCV Id: RCV001063824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362534.1:p.Phe392Leu
CA55351063
NM_001375605.1:c.1176C>A
CA348405701
NM_001375605.1:c.1174T>C
CA348405706
NM_001375605.1:c.1176C>G