Canonical Allele Identifier: PA2827971689
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2576Asn
CA16038277
NM_001354898.2:c.7727G>A