Canonical Allele Identifier: PA2825636960
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1483673
ClinVar RCV Id: RCV002025495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr46Ala
CA360612107
NM_001127511.3:c.136A>G