Canonical Allele Identifier: PA2825014715
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys398Arg
CA026866
NM_000038.6:c.1193A>G