Canonical Allele Identifier: PA2825640088
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp1115Val
CA16028781
NM_001127511.3:c.3344A>T