Canonical Allele Identifier: PA2828018170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188207
ClinVar RCV Id: RCV000168132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser623Ala
CA007751
NM_001354906.2:c.1867T>G