ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828036939
Gene: VCP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
425845
ClinVar RCV:
RCV000498690
RCV003766796
ClinVar Variation:
432305
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341856.1:p.Gly83Ala
CA373291969
NM_001354927.2:c.248G>C