Canonical Allele Identifier: PA2826210320
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 338933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182606.1:p.Pro86Ser
CA9924316
NM_001195677.2:c.256C>T