ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825055030
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1399364
ClinVar RCV Id:
RCV002282639
RCV001917627
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Ala1399Val
CA397483613
NM_000135.4:c.4196C>T