ClinGen Allele Registry
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Canonical Allele Identifier:
PA916015060
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000472481
RCV001276510
RCV001509531
RCV001821268
ClinVar Variation:
408205
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Arg1053Cys
CA8251319
NM_001286167.3:c.3157C>T