Canonical Allele Identifier: PA2826210286
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 534272
ClinVar RCV Id: RCV002254563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182606.1:p.Pro35Leu
CA409442392
NM_001195677.2:c.104C>T