ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916015217
Gene: FANCA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
554887
ClinVar RCV Id:
RCV000670597
RCV000801328
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001273096.1:p.Ser1401Leu
CA8250693
NM_001286167.3:c.4202C>T