Canonical Allele Identifier: PA2828023349
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1588Asn
CA040545
NM_001354903.2:c.4763C>A