Canonical Allele Identifier: PA2828037308
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser1002Cys
CA035180
NM_001354904.2:c.3005C>G