Canonical Allele Identifier: PA174751
Gene: BEND5 HGNC NCBI

Linked Data

ClinVar Variation Id: 161769
ClinVar RCV Id: RCV000149305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078879.2:p.Ile404Val
CA174750
NM_024603.4:c.1210A>G