Canonical Allele Identifier: PA2827964205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser268Asn
CA16023237
NM_001354898.2:c.803G>A