Canonical Allele Identifier: PA2828014187
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser130Gly
CA008731
NM_001354903.2:c.388A>G