Canonical Allele Identifier: PA2827996007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1633Arg
CA16032428
NM_001354901.2:c.4898C>G