Canonical Allele Identifier: PA2827973684
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys370Arg
CA026866
NM_001354899.2:c.1109A>G