Canonical Allele Identifier: PA2828023136
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_001341832.1:p.Ser1557Arg
CA16032213
NM_001354903.2:c.4669A>C
CA16032219
NM_001354903.2:c.4671T>A
CA16032220
NM_001354903.2:c.4671T>G