Canonical Allele Identifier: PA2828477097
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456361
ClinVar RCV Id: RCV000538452 RCV001150741 RCV001821498 RCV001528593 RCV003979943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361183.1:p.Gln26His
CA2249106
NM_001374254.1:c.78A>C
CA351717922
NM_001374254.1:c.78A>T