Canonical Allele Identifier: PA645401036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile2071Met
CA10578423
NM_001127510.3:c.6213A>G