Canonical Allele Identifier: PA2828051902
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822781
ClinVar RCV Id: RCV001018420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser236Arg
CA16023248
NM_001354905.2:c.706A>C
CA16023252
NM_001354905.2:c.708T>A
CA16023253
NM_001354905.2:c.708T>G