Canonical Allele Identifier: PA2828004097
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp2399Val
CA048153
NM_001354902.2:c.7196A>T