Canonical Allele Identifier: PA2828023268
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1433Ser
CA040767
NM_001354906.2:c.4298A>G