Canonical Allele Identifier: PA2828029252
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2335Ser
CA16038396
NM_001354906.2:c.7004A>G