Canonical Allele Identifier: PA2828012048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro2391Ala
CA013688
NM_001354902.2:c.7171C>G