Canonical Allele Identifier: PA2827999892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu103Val
CA033407
NM_001354902.2:c.307C>G