Canonical Allele Identifier: PA2580260797
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718025
ClinVar RCV Id: RCV002299570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Gln28His
CA352228483
NM_001904.4:c.84G>C
CA352228484
NM_001904.4:c.84G>T