ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826710757
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
467218
ClinVar RCV:
RCV000552747
ClinVar Variation:
456102
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.His89Tyr
CA8253102
NM_001286167.3:c.265C>T