Canonical Allele Identifier: PA2827952006
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1742135
ClinVar RCV Id: RCV002330441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1566Lys
CA16031507
NM_001354896.2:c.4698C>A
CA16031508
NM_001354896.2:c.4698C>G