Canonical Allele Identifier: PA2827943000
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1128Cys
CA035180
NM_001354895.2:c.3383C>G