Canonical Allele Identifier: PA2828010635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1995Ala
CA044235
NM_001354902.2:c.5983C>G