Canonical Allele Identifier: PA2828007204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 928193
ClinVar RCV Id: RCV001191960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser1498Arg
CA16032213
NM_001354905.2:c.4492A>C
CA16032219
NM_001354905.2:c.4494T>A
CA16032220
NM_001354905.2:c.4494T>G