Canonical Allele Identifier: PA2828027236
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2037Ser
CA012700
NM_001354906.2:c.6109C>T