Canonical Allele Identifier: PA2827986840
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 928193
ClinVar RCV Id: RCV001191960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser1617Arg
CA16032213
NM_001354900.2:c.4849A>C
CA16032219
NM_001354900.2:c.4851T>A
CA16032220
NM_001354900.2:c.4851T>G