Canonical Allele Identifier: PA2741811789
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2721366
ClinVar RCV Id: RCV003522385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Thr1397Lys
CA397483675
NM_000135.4:c.4190C>A