Canonical Allele Identifier: PA2825014672
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1739989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile391Ser
CA16023873
NM_000038.6:c.1172T>G