Canonical Allele Identifier: PA2827964217
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser271Asn
CA16023257
NM_001354898.2:c.812G>A