Canonical Allele Identifier: PA2827975659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Tyr1003Cys
CA16028105
NM_001354899.2:c.3008A>G