Canonical Allele Identifier: PA2825641847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1679Ala
CA10578392
NM_001127511.3:c.5035A>G