Canonical Allele Identifier: PA2827980789
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu2551Lys
CA16038126
NM_001354899.2:c.7651G>A