Canonical Allele Identifier: PA2827982508
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser247Gly
CA16023315
NM_001354900.2:c.739A>G