Canonical Allele Identifier: PA2828012270
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp2330Val
CA048153
NM_001354905.2:c.6989A>T