Canonical Allele Identifier: PA658806701
Gene: NCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 500837
ClinVar RCV Id: RCV000595538 RCV000968901 RCV001509096 RCV003905544
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_038202.2:p.Arg58Cys
CA10212881
NM_013416.4:c.172C>T