Canonical Allele Identifier: PA2825329808
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 456349
ClinVar RCV Id: RCV000539433 RCV000987093 RCV001144633 RCV001531560 RCV003151085 RCV003942731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018125.1:p.Thr61Met
CA2249126
NM_001018115.2:c.182C>T