Canonical Allele Identifier: PA916015218
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408170
ClinVar RCV Id: RCV000458944 RCV000765320 RCV001252734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1410Leu
CA8250683
NM_001286167.3:c.4229C>T