Canonical Allele Identifier: PA2828028435
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp2207Val
CA048153
NM_001354906.2:c.6620A>T