Canonical Allele Identifier: PA2825648767
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 847320
ClinVar RCV Id: RCV001050845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121123.1:p.Trp22Arg
CA343684969
NM_001127651.3:c.64T>C
CA343684977
NM_001127651.3:c.64T>A