ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014881
Gene: FANCA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
374789
ClinVar RCV:
RCV000432541
ClinVar Variation:
384094
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Pro497Ser
CA16607150
NM_001286167.3:c.1489C>T