Canonical Allele Identifier: PA2825644330
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2478Gln
CA16037618
NM_001127511.3:c.7434T>A
CA16037619
NM_001127511.3:c.7434T>G