Canonical Allele Identifier: PA2827940658
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231519
ClinVar RCV Id: RCV004525590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His388Gln
CA16023852
NM_001354895.2:c.1164C>A
CA16023853
NM_001354895.2:c.1164C>G