Canonical Allele Identifier: PA916014933
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134250
ClinVar RCV Id: RCV000120923 RCV000707539 RCV001271604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asn691Ser
CA159263
NM_001286167.3:c.2072A>G