Canonical Allele Identifier: PA110846
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134264
ClinVar RCV Id: RCV000120937 RCV000351747 RCV000488415 RCV001094408 RCV001705888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ser1088Phe
CA159302
NM_000135.4:c.3263C>T