Canonical Allele Identifier: PA2828015117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser295Gly
CA015623
NM_001354903.2:c.883A>G