Canonical Allele Identifier: PA2828997837
Gene: BANP HGNC NCBI

Linked Data

ClinVar Variation Id: 487782
ClinVar RCV Id: RCV000577856
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371867.1:p.Asn198Ser
CA397045705
NM_001384938.1:c.593A>G