Canonical Allele Identifier: PA2827971541
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2531Leu
CA048890
NM_001354898.2:c.7592C>T