Canonical Allele Identifier: PA2825633380
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 928193
ClinVar RCV Id: RCV001191960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1658Arg
CA16032213
NM_001127510.3:c.4972A>C
CA16032219
NM_001127510.3:c.4974T>A
CA16032220
NM_001127510.3:c.4974T>G