Canonical Allele Identifier: PA2827968589
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 928193
ClinVar RCV Id: RCV001191960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1633Arg
CA16032213
NM_001354898.2:c.4897A>C
CA16032219
NM_001354898.2:c.4899T>A
CA16032220
NM_001354898.2:c.4899T>G