ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA159345
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
134280
ClinVar RCV Id:
RCV000120953
RCV000666660
RCV000824570
RCV003477510
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000126.2:p.Leu1339Phe
CA159343
NM_000135.4:c.4015C>T