Canonical Allele Identifier: PA2827986933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1648Asn
CA040545
NM_001354900.2:c.4943C>A