Canonical Allele Identifier: PA2825021393
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1709Ser
CA16032532
NM_000038.6:c.5125A>T
CA16032534
NM_000038.6:c.5126C>G