Canonical Allele Identifier: PA2828002191
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Lys1346Arg
CA038588
NM_001354902.2:c.4037A>G