Canonical Allele Identifier: PA355961
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1761Ser
CA041233
NM_000038.6:c.5282A>G