Canonical Allele Identifier: PA2828024012
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 950861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro1677Leu
CA16032992
NM_001354903.2:c.5030C>T