Canonical Allele Identifier: PA2827977744
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2726917
ClinVar RCV Id: RCV003539016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1624Ala
CA16032181
NM_001354899.2:c.4870T>G