Canonical Allele Identifier: PA2827942992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1126Cys
CA16028731
NM_001354895.2:c.3376A>T