Canonical Allele Identifier: PA2829679836
Gene: SPTBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2220649
ClinVar RCV Id: RCV002701889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008877.2:p.Met1510Thr
CA381469818
NM_006946.4:c.4529T>C