Canonical Allele Identifier: PA2825638081
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411398
ClinVar Variation Id: 485101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His426Gln
CA027188
NM_001127511.3:c.1278T>G
CA16024222
NM_001127511.3:c.1278T>A