Canonical Allele Identifier: PA2825022491
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1993Ser
CA16034417
NM_000038.6:c.5977C>T