Canonical Allele Identifier: PA2828002881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1670Ser
CA041233
NM_001354902.2:c.5009A>G