Canonical Allele Identifier: PA658660783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2571_Ser2572del
CA048994
NM_001127510.3:c.7711_7716del