Canonical Allele Identifier: PA2827963993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg205His
CA012635
NM_001354898.2:c.614G>A