Canonical Allele Identifier: PA2828012829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2418Pro
CA16038121
NM_001354905.2:c.7252T>C