Canonical Allele Identifier: PA2827982755
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1739989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile332Ser
CA16023873
NM_001354900.2:c.995T>G