Canonical Allele Identifier: PA2828568157
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 372807
ClinVar RCV Id: RCV000413659 RCV003144247
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362209.1:p.Asn151Ser
CA3042272
NM_001375280.1:c.452A>G