Canonical Allele Identifier: PA2828004912
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Tyr106Cys
CA033841
NM_001354902.2:c.317A>G