Canonical Allele Identifier: PA658659329
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu656Val
CA030483
NM_001127510.3:c.1966C>G