Canonical Allele Identifier: PA2827989499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2427Pro
CA013665
NM_001354900.2:c.7279T>C