Canonical Allele Identifier: PA658820174
Gene: VAPB HGNC NCBI

Linked Data

ClinVar Variation Id: 534272
ClinVar RCV Id: RCV002254563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004729.1:p.Pro35Leu
CA409442392
NM_004738.5:c.104C>T