Canonical Allele Identifier: PA2825014182
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu304Pro
CA16023306
NM_000038.6:c.911T>C