Canonical Allele Identifier: PA2828047792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp2364Val
CA048153
NM_001354904.2:c.7091A>T