Canonical Allele Identifier: PA916015008
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203995
ClinVar RCV Id: RCV000239379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Lys921Ile
CA10575737
NM_001286167.3:c.2762A>T