Canonical Allele Identifier: PA159518
Gene: FANCD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134329
ClinVar RCV Id: RCV000121003 RCV000630963 RCV003315755 RCV003905154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149075.2:p.Pro1466Thr
CA159516
NM_033084.6:c.4396C>A