ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA097472
Gene: VAPB
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
39467
ClinVar RCV:
RCV000023467
RCV000059634
ClinVar Variation:
30510
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004729.1:p.Thr46Ile
CA219846
NM_004738.5:c.137C>T