Canonical Allele Identifier: PA16040142
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu2619Ala
CA10578452
NM_000038.6:c.7856A>C