ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658661119
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
456139
ClinVar RCV Id:
RCV000532298
RCV000764090
RCV001797096
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.His292Asp
CA8252711
NM_000135.4:c.874C>G