Canonical Allele Identifier: PA2827995705
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala1536Ser
CA16031815
NM_001354901.2:c.4606G>T