Canonical Allele Identifier: PA2828011990
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2377Pro
CA013665
NM_001354902.2:c.7129T>C