Canonical Allele Identifier: PA2828023537
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1524741
ClinVar RCV Id: RCV003773518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1617Ser
CA16032593
NM_001354903.2:c.4849G>T