ClinGen Allele Registry
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Canonical Allele Identifier:
PA916015107
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
138007
ClinVar RCV:
RCV000120941
RCV000226225
RCV001843480
RCV003147340
RCV003477506
RCV003935154
ClinVar Variation:
134268
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Pro1175Leu
CA159313
NM_001286167.3:c.3524C>T