Canonical Allele Identifier: PA2573089307
Gene: SPTBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 226117
ClinVar RCV Id: RCV000211499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008877.2:p.Ile157Thr
CA10576252
NM_006946.4:c.470T>C