Canonical Allele Identifier: PA2827989886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala2543Ser
CA16038165
NM_001354900.2:c.7627G>T