Canonical Allele Identifier: PA2825635989
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2105910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr310Ser
CA16023339
NM_001127510.3:c.928A>T
CA16023341
NM_001127510.3:c.929C>G