ClinGen Allele Registry
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Canonical Allele Identifier:
PA916015204
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
134280
ClinVar RCV Id:
RCV000120953
RCV000666660
RCV000824570
RCV003477510
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Leu1339Phe
CA159343
NM_001286167.3:c.4015C>T