Canonical Allele Identifier: PA2827964026
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr215Arg
CA047191
NM_001354898.2:c.644C>G