Canonical Allele Identifier: PA645429998
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 246612
ClinVar RCV Id: RCV000236495 RCV000503767 RCV000721015 RCV003930015 RCV001727653 RCV003316313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Gly666Ser
CA10352977
NM_001018113.2:c.1996G>A