Canonical Allele Identifier: PA2827999213
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2606Ser
CA16038695
NM_001354901.2:c.7816C>T