Canonical Allele Identifier: PA2828997700
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_001371858.1:p.Asn237Ser
CA397045705
NM_001384929.1:c.710A>G