Canonical Allele Identifier: PA2828009748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 950861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1687Leu
CA16032992
NM_001354902.2:c.5060C>T