Canonical Allele Identifier: PA645400210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1700Val
CA10578393
NM_001127510.3:c.5099C>T