ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014982
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000199923
RCV000674142
RCV001091062
RCV002252053
ClinVar Variation:
215981
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Gln869Pro
CA338977
NM_001286167.3:c.2606A>C