Canonical Allele Identifier: PA2828567646
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 420176
ClinVar RCV Id: RCV000479573 RCV001150340 RCV002489157
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362207.1:p.Val152Met
CA3042270
NM_001375278.1:c.454G>A