Canonical Allele Identifier: PA164018
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val2716Met
CA014393
NM_001127510.3:c.8146G>A