Canonical Allele Identifier: PA2828044608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220442
ClinVar Variation Id: 470028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp1868Glu
CA043621
NM_001354904.2:c.5604C>G
CA16034426
NM_001354904.2:c.5604C>A