Canonical Allele Identifier: PA2825640116
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2158192
ClinVar RCV Id: RCV003653654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1122Leu
CA16028830
NM_001127511.3:c.3365C>T