Canonical Allele Identifier: PA2825638609
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu611Ser
CA16025442
NM_001127511.3:c.1832T>C