Canonical Allele Identifier: PA2827959797
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1900687
ClinVar RCV Id: RCV003776566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1770Ser
CA16032868
NM_001354897.2:c.5308C>T