Canonical Allele Identifier: PA658660267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1993Ser
CA16034417
NM_001127510.3:c.5977C>T