Canonical Allele Identifier: PA2828046942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2243Ser
CA046951
NM_001354904.2:c.6727C>T