Canonical Allele Identifier: PA2828030264
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2827950
ClinVar RCV Id: RCV003744279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn2643Lys
CA16039202
NM_001354903.2:c.7929T>A
CA16039203
NM_001354903.2:c.7929T>G