Canonical Allele Identifier: PA2825636189
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2627Thr
CA16038450
NM_001127510.3:c.7879T>A