Canonical Allele Identifier: PA2827979851
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2268Asn
CA16036358
NM_001354899.2:c.6803G>A