Canonical Allele Identifier: PA2828019775
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu1028Ser
CA008351
NM_001354903.2:c.3083T>C