Canonical Allele Identifier: PA2825634847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587029
ClinVar RCV Id: RCV003339110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2361Pro
CA16036756
NM_001127510.3:c.7081T>C