Canonical Allele Identifier: PA645402334
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu2619Ala
CA10578452
NM_001127510.3:c.7856A>C