Canonical Allele Identifier: PA2825636966
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2750901
ClinVar RCV Id: RCV003536704

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser47del
CA1573442785
NM_001127511.3:c.139_141del