Canonical Allele Identifier: PA2499241599
Gene: NCF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010288
ClinVar RCV Id: RCV001307894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177723.1:p.Met46Ile
CA343684313
NM_001190794.2:c.138G>A
CA343684317
NM_001190794.2:c.138G>C
CA343684319
NM_001190794.2:c.138G>T