Canonical Allele Identifier: PA658825709
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 554887
ClinVar RCV Id: RCV000670597 RCV000801328
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg1400Cys
CA8250693
NM_000135.4:c.4198C>T