Canonical Allele Identifier: PA2827994142
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1069Cys
CA035180
NM_001354901.2:c.3206C>G