Canonical Allele Identifier: PA2828019769
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser1027Cys
CA035180
NM_001354903.2:c.3080C>G