Canonical Allele Identifier: PA916042181
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg240His
CA012635
NM_001354902.2:c.719G>A