ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825524782
Gene: CTNNB1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000419361
RCV000420492
RCV000420998
RCV000421620
RCV000429634
RCV000430785
RCV000431858
RCV000432982
RCV000438660
RCV000441059
RCV000441660
ClinVar Variation:
375894
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001091679.1:p.Ser37Tyr
CA16602377
NM_001098209.1:c.110C>A