Canonical Allele Identifier: PA2825644253
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2453Leu
CA10578443
NM_001127511.3:c.7358C>T