Canonical Allele Identifier: PA2828014451
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser13Asn
CA16023257
NM_001354906.2:c.38G>A