ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014916
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
530733
ClinVar RCV:
RCV000630927
RCV001120168
RCV001771851
RCV003945583
ClinVar Variation:
526402
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Ala635Val
CA8251971
NM_001286167.3:c.1904C>T