Canonical Allele Identifier: PA915968026
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2246
ClinVar RCV Id: RCV000002334
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121123.1:p.Ala128Val
CA115433
NM_001127651.3:c.383C>T