Canonical Allele Identifier: PA2825024180
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2425Asn
CA16037169
NM_000038.6:c.7274G>A