Canonical Allele Identifier: PA2828029366
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn2517Ser
CA16038396
NM_001354903.2:c.7550A>G