Canonical Allele Identifier: PA215459
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser130Gly
CA008731
NM_000038.6:c.388A>G