Canonical Allele Identifier: PA2828005299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr320Ser
CA16023339
NM_001354902.2:c.958A>T
CA16023341
NM_001354902.2:c.959C>G