Canonical Allele Identifier: PA916014930
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526387
ClinVar RCV Id: RCV000630911 RCV001271605 RCV001756040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Val677Met
CA8251928
NM_001286167.3:c.2029G>A