Canonical Allele Identifier: PA2827978868
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1965Ser
CA16034417
NM_001354899.2:c.5893C>T