Canonical Allele Identifier: PA2825634880
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 852832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2377His
CA16036858
NM_001127510.3:c.7129A>C