Canonical Allele Identifier: PA2827990130
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462
ClinVar RCV Id: RCV003476609 RCV003745601
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2618Leu
CA16038652
NM_001354900.2:c.7852G>C
CA16038653
NM_001354900.2:c.7852G>T