Canonical Allele Identifier: PA2827990176
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2631Val
CA16038743
NM_001354900.2:c.7892G>T