ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014792
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000274943
RCV001094307
RCV001820959
RCV003922359
ClinVar Variation:
321366
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Val230Ile
CA8252857
NM_001286167.3:c.688G>A