Canonical Allele Identifier: PA2826210301
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 4806
ClinVar RCV Id: RCV000005073 RCV000059635 RCV002254542 RCV002254541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182606.1:p.Pro56Ser
CA117096
NM_001195677.2:c.166C>T