Canonical Allele Identifier: PA2828013370
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2505Ser
CA16038695
NM_001354905.2:c.7513C>T