Canonical Allele Identifier: PA2825644827
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val2641Leu
CA16038652
NM_001127511.3:c.7921G>C
CA16038653
NM_001127511.3:c.7921G>T