Canonical Allele Identifier: PA645400208
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1697Ala
CA10578392
NM_001127510.3:c.5089A>G