Canonical Allele Identifier: PA2825055018
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1710975
ClinVar RCV Id: RCV002292262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro1392Ser
CA397483811
NM_000135.4:c.4174C>T