Canonical Allele Identifier: PA2827961663
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2340Phe
CA16036569
NM_001354897.2:c.7019C>T