Canonical Allele Identifier: PA2825629578
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1005Val
CA10578347
NM_001127510.3:c.3014C>T