Canonical Allele Identifier: PA2828048757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2492Ser
CA16038396
NM_001354904.2:c.7475A>G