Canonical Allele Identifier: PA2827980271
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2393Leu
CA047405
NM_001354899.2:c.7178C>T