Canonical Allele Identifier: PA2828035330
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser717Gly
CA032383
NM_001354904.2:c.2149A>G