Canonical Allele Identifier: PA2827972335
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2774Pro
CA16039553
NM_001354898.2:c.8320T>C