Canonical Allele Identifier: PA645404513
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237050
ClinVar RCV Id: RCV000232454 RCV000765323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Cys1159Ser
CA8251141
NM_000135.4:c.3476G>C
CA397485896
NM_000135.4:c.3475T>A