Canonical Allele Identifier: PA2827984213
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro824Ser
CA007632
NM_001354900.2:c.2470C>T