ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014963
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
401430
ClinVar RCV:
RCV000458018
RCV001274572
ClinVar Variation:
408167
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Gly811Asp
CA8251729
NM_001286167.3:c.2432G>A