Canonical Allele Identifier: PA2828004542
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2827950
ClinVar RCV Id: RCV003744279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2653Lys
CA16039202
NM_001354902.2:c.7959T>A
CA16039203
NM_001354902.2:c.7959T>G