Canonical Allele Identifier: PA2826710835
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408207
ClinVar RCV Id: RCV000464585 RCV001276567 RCV002264943 RCV002526413 RCV003902647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Thr126Met
CA8253048
NM_001286167.3:c.377C>T