Canonical Allele Identifier: PA2825024586
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2531Ala
CA16037824
NM_000038.6:c.7591T>G