Canonical Allele Identifier: PA2825018738
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 849086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1107Val
CA16028617
NM_000038.6:c.3320C>T