Canonical Allele Identifier: PA916040500
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1707Asn
CA040545
NM_001354896.2:c.5120C>A