Canonical Allele Identifier: PA2827996308
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 950861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1719Leu
CA16032992
NM_001354901.2:c.5156C>T