Canonical Allele Identifier: PA2828016669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.His551Gln
CA16025592
NM_001354903.2:c.1653C>A
CA16025593
NM_001354903.2:c.1653C>G