Canonical Allele Identifier: PA2825644492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2534Cys
CA16037960
NM_001127511.3:c.7600A>T