Canonical Allele Identifier: PA1139734945
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 925531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser306Thr
CA16023258
NM_001354902.2:c.917G>C