Canonical Allele Identifier: PA2825641827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1673Leu
CA16032423
NM_001127511.3:c.5018C>T