Canonical Allele Identifier: PA658660194
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1843Thr
CA16033423
NM_001127510.3:c.5527C>A