Canonical Allele Identifier: PA2827998950
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala2525Ser
CA16038165
NM_001354901.2:c.7573G>T