Canonical Allele Identifier: PA2828016467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954
ClinVar RCV Id: RCV000222920 RCV003335256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser351Arg
CA10578330
NM_001354906.2:c.1053T>G
CA16025473
NM_001354906.2:c.1051A>C
CA16025479
NM_001354906.2:c.1053T>A