Canonical Allele Identifier: PA2828030813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2730Leu
CA050906
NM_001354903.2:c.8189C>T