Canonical Allele Identifier: PA215544
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2586Ile
CA014009
NM_000038.6:c.7757G>T