Canonical Allele Identifier: PA916014834
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456146
ClinVar RCV Id: RCV000548806 RCV000674060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.His322Tyr
CA8252610
NM_001286167.3:c.964C>T