Canonical Allele Identifier: PA2828013059
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2458Ser
CA16038396
NM_001354905.2:c.7373A>G