Canonical Allele Identifier: PA2828024351
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1728Ser
CA042093
NM_001354903.2:c.5183A>G