Canonical Allele Identifier: PA1139687016
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 836067
ClinVar RCV Id: RCV001037102 RCV001274512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gly1391Arg
CA8250766
NM_001286167.3:c.4171G>A
CA397484242
NM_001286167.3:c.4171G>C