Canonical Allele Identifier: PA2825644322
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1470437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu2475Val
CA16037597
NM_001127511.3:c.7423C>G