Canonical Allele Identifier: PA338303
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 216278
ClinVar RCV Id: RCV000198937 RCV000765322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gln1235Glu
CA338301
NM_000135.4:c.3703C>G