ClinGen Allele Registry
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Canonical Allele Identifier:
PA916015215
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000493395
RCV001834601
ClinVar Variation:
429862
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Thr1373Ala
CA8250780
NM_001286167.3:c.4117A>G