Canonical Allele Identifier: PA2825629731
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727379
ClinVar RCV Id: RCV002319894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1028Gly
CA16028082
NM_001127510.3:c.3082A>G