Canonical Allele Identifier: PA2827956728
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser853Gly
CA032383
NM_001354897.2:c.2557A>G