Canonical Allele Identifier: PA645400226
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1721Asp
CA10578397
NM_001127510.3:c.5162G>A