Canonical Allele Identifier: PA2825638884
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Tyr719His
CA031174
NM_001127511.3:c.2155T>C