Canonical Allele Identifier: PA332311
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser295Gly
CA015623
NM_001127510.3:c.883A>G