Canonical Allele Identifier: PA2573089326
Gene: SPTBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64368
ClinVar RCV Id: RCV000054554 RCV001568501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008877.2:p.Arg480Trp
CA264227
NM_006946.4:c.1438C>T