Canonical Allele Identifier: PA2828014306
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2671Leu
CA050906
NM_001354905.2:c.8012C>T