Canonical Allele Identifier: PA2580193372
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2153801
ClinVar RCV Id: RCV003081462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Glu923Val
CA286555314
NM_001286167.3:c.2768A>T