Canonical Allele Identifier: PA2827353077
Gene: CFI HGNC NCBI

Linked Data

ClinVar Variation Id: 2724049
ClinVar RCV Id: RCV003561571
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317964.1:p.Glu541Asp
CA357854474
NM_001331035.2:c.1623A>T
CA357854475
NM_001331035.2:c.1623A>C