Canonical Allele Identifier: PA332309
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser277Gly
CA015623
NM_001127511.3:c.829A>G