Canonical Allele Identifier: PA2499228741
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1000018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ile1396Met
CA397483690
NM_000135.4:c.4188A>G