Canonical Allele Identifier: PA2827990183
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2633Pro
CA16038751
NM_001354900.2:c.7897T>C