Canonical Allele Identifier: PA2827949807
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1739989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile391Ser
CA16023873
NM_001354896.2:c.1172T>G