Canonical Allele Identifier: PA2573089307
Gene: SPTBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 226117
ClinVar RCV Id: RCV000211499
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Amino-acid Alleles

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