Canonical Allele Identifier: PA658662348
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 456183
ClinVar RCV Id: RCV000528766 RCV001169617 RCV001169618 RCV001444357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Ala776Val
CA10352926
NM_001018113.2:c.2327C>T