Canonical Allele Identifier: PA2828042313
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2707798
ClinVar RCV Id: RCV003536455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr1571Ile
CA16032461
NM_001354904.2:c.4712C>T