Canonical Allele Identifier: PA2828009442
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1600Leu
CA16032423
NM_001354902.2:c.4799C>T