Canonical Allele Identifier: PA2825633526
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1728Val
CA040889
NM_001127510.3:c.5182A>G