Canonical Allele Identifier: PA156897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41509

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln203Glu
CA010884
NM_001127510.3:c.607C>G