Canonical Allele Identifier: PA2828476282
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 342370
ClinVar RCV Id: RCV000383944 RCV000504499 RCV001094917 RCV003950197 RCV003229830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361182.1:p.Lys834Asn
CA2250142
NM_001374253.1:c.2502A>C
CA351742296
NM_001374253.1:c.2502A>T