Canonical Allele Identifier: PA156801
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2328Ser
CA012759
NM_001127511.3:c.6982C>T