Canonical Allele Identifier: PA2741951925
Gene: STAB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2554118
ClinVar RCV Id: RCV004326645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055951.2:p.Ala629Val
CA2440749
NM_015136.3:c.1886C>T