Canonical Allele Identifier: PA2828011522
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2219Ser
CA047031
NM_001354905.2:c.6656C>G
CA16036872
NM_001354905.2:c.6655A>T