Canonical Allele Identifier: PA2827954448
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala71Thr
CA006037
NM_001354897.2:c.211G>A