Canonical Allele Identifier: PA2825014222
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His307Gln
CA16023326
NM_000038.6:c.921T>A
CA16023327
NM_000038.6:c.921T>G