Canonical Allele Identifier: PA2825643963
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2361Ser
CA047031
NM_001127511.3:c.7082C>G
CA16036872
NM_001127511.3:c.7081A>T