Canonical Allele Identifier: PA645429972
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 408161
ClinVar RCV Id: RCV000472221 RCV001821264 RCV003258818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Ile170Met
CA16616639
NM_001018113.2:c.510T>G