Canonical Allele Identifier: PA1139687026
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 974171
ClinVar RCV Id: RCV001256420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser1400Thr
CA286614345
NM_001286167.3:c.4199G>C