Canonical Allele Identifier: PA2827992655
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn601Ser
CA16025642
NM_001354901.2:c.1802A>G