Canonical Allele Identifier: PA2829076739
Gene: BANP HGNC NCBI

Linked Data

ClinVar Variation Id: 487782
ClinVar RCV Id: RCV000577856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373921.1:p.Asn231Ser
CA397045705
NM_001386992.1:c.692A>G