Canonical Allele Identifier: PA2825017004
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser843Gly
CA032383
NM_000038.6:c.2527A>G