Canonical Allele Identifier: PA2828027655
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2096Ser
CA047031
NM_001354906.2:c.6287C>G
CA16036872
NM_001354906.2:c.6286A>T