Canonical Allele Identifier: PA2825014971
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411398
ClinVar Variation Id: 485101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His444Gln
CA027188
NM_000038.6:c.1332T>G
CA16024222
NM_000038.6:c.1332T>A