Canonical Allele Identifier: PA645403607
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 338930
ClinVar RCV Id: RCV000312731 RCV000348929 RCV002254546 RCV002323548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004729.1:p.Pro111Leu
CA9924233
NM_004738.5:c.332C>T