ClinGen Allele Registry
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Canonical Allele Identifier:
PA127276
Gene: CTNNB1
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000019147
RCV000019148
RCV000418596
RCV000420986
RCV000421635
RCV000423964
RCV000428161
RCV000434049
RCV000437352
RCV000438845
RCV000439964
RCV000443180
RCV000505658
RCV003332083
ClinVar Variation:
17583
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001895.1:p.Ser33Phe
CA127275
NM_001904.4:c.98C>T