Canonical Allele Identifier: PA174751
Gene: BEND5 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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