Canonical Allele Identifier: PA2828476961
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456359
ClinVar RCV Id: RCV000550015 RCV001770410 RCV003237893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361182.1:p.Thr1314Met
CA2250621
NM_001374253.1:c.3941C>T