Canonical Allele Identifier: PA2825019327
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His1210Leu
CA035977
NM_000038.6:c.3629A>T