ClinGen Allele Registry
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Canonical Allele Identifier:
PA916031225
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
134277
ClinVar RCV Id:
RCV000120950
RCV000537860
RCV003144133
RCV003477509
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001338759.1:p.Ser103Leu
CA159334
NM_001351830.2:c.308C>T