Canonical Allele Identifier: PA245170
Gene: FANCB HGNC NCBI

Linked Data

ClinVar Variation Id: 197175
ClinVar RCV Id: RCV000178139 RCV001085637 RCV001818433 RCV003967429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018123.1:p.Ile330Thr
CA245168
NM_001018113.2:c.989T>C