Canonical Allele Identifier: PA2827988646
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141618
ClinVar RCV Id: RCV000130211 RCV000409211 RCV000484737 RCV000765788 RCV001157265 RCV002222403 RCV003650393
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met2172Ile
CA012330
NM_001354900.2:c.6516G>A
CA16035852
NM_001354900.2:c.6516G>C
CA16035853
NM_001354900.2:c.6516G>T