Canonical Allele Identifier: PA294306
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro865Ser
CA007632
NM_001127510.3:c.2593C>T