ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014806
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
489977
ClinVar RCV:
RCV000593561
RCV001243169
RCV002483594
ClinVar Variation:
498553
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Glu260Lys
CA8252812
NM_001286167.3:c.778G>A