Canonical Allele Identifier: PA2825012640
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly122Val
CA036174
NM_000038.6:c.365G>T