Canonical Allele Identifier: PA2827965819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu806Ser
CA10582297
NM_001354898.2:c.2417T>C