Canonical Allele Identifier: PA2826714579
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456127
ClinVar RCV Id: RCV000534717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ala1405Val
CA397483486
NM_001286167.3:c.4214C>T