ClinGen Allele Registry
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Canonical Allele Identifier:
PA658800262
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
530538
ClinVar RCV:
RCV000630847
RCV001121953
RCV003237964
ClinVar Variation:
526331
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Pro1213Ala
CA8251038
NM_000135.4:c.3637C>G