Canonical Allele Identifier: PA2499245608
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1047089
ClinVar RCV Id: RCV001351754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asn644Lys
CA397450252
NM_001286167.3:c.1932C>G
CA397450255
NM_001286167.3:c.1932C>A