Canonical Allele Identifier: PA658660805
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His2591Pro
CA049129
NM_001127510.3:c.7772A>C