Canonical Allele Identifier: PA2825330618
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_001018125.1:p.Thr1351Met
CA2250621
NM_001018115.2:c.4052C>T