Canonical Allele Identifier: PA2825644712
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2606Lys
CA16038436
NM_001127511.3:c.7818T>A
CA16038437
NM_001127511.3:c.7818T>G