ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916051523
Gene: FANCB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
435140
ClinVar RCV Id:
RCV000501276
RCV001516277
RCV003237883
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_689846.1:p.Leu43Ile
CA10353231
NM_152633.4:c.127T>A