Canonical Allele Identifier: PA2825629722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1026Ser
CA16028071
NM_001127510.3:c.3077A>G