Canonical Allele Identifier: PA2827991590
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His248Gln
CA16023326
NM_001354901.2:c.744T>A
CA16023327
NM_001354901.2:c.744T>G