Canonical Allele Identifier: PA916015107
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134268
ClinVar RCV Id: RCV000120941 RCV000226225 RCV001843480 RCV003147340 RCV003477506 RCV003935154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Pro1175Leu
CA159313
NM_001286167.3:c.3524C>T