Canonical Allele Identifier: PA2828052126
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr251Ser
CA16023339
NM_001354905.2:c.751A>T
CA16023341
NM_001354905.2:c.752C>G