Canonical Allele Identifier: PA2827946552
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Glu2208Ala
CA045546
NM_001354895.2:c.6623A>C