Canonical Allele Identifier: PA286536
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127279
ClinVar RCV Id: RCV000115071
ClinVar Variation Id: 628655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile620Leu
CA006331
NM_001127511.3:c.1858A>T
CA16025497
NM_001127511.3:c.1858A>C