Canonical Allele Identifier: PA2828027322
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2195Asn
CA16036358
NM_001354903.2:c.6584G>A