Canonical Allele Identifier: PA1139671057
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 955590
ClinVar RCV Id: RCV001228261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ile1396Leu
CA397483705
NM_000135.4:c.4186A>T
CA397483711
NM_000135.4:c.4186A>C