Canonical Allele Identifier: PA2828009436
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1598Asn
CA040545
NM_001354902.2:c.4793C>A