Canonical Allele Identifier: PA1139733691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro41Leu
CA16042079
NM_001354902.2:c.122C>T