ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA105948
Gene: STUB1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
212325
ClinVar RCV Id:
RCV000194931
RCV000989407
RCV002517140
RCV002517982
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005852.2:p.Lys145Gln
CA209422
NM_005861.4:c.433A>C