Canonical Allele Identifier: PA189361
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn741Ser
CA007300
NM_000038.6:c.2222A>G