Canonical Allele Identifier: PA2827968683
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1664Asn
CA040545
NM_001354898.2:c.4991C>A