Canonical Allele Identifier: PA2827975669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716842
ClinVar RCV Id: RCV003743862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu1006Asp
CA16028128
NM_001354899.2:c.3018G>C
CA16028129
NM_001354899.2:c.3018G>T