Canonical Allele Identifier: PA2827982938
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230838
ClinVar RCV Id: RCV000217057 RCV000585258 RCV002494587 RCV003475011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln386Glu
CA10578313
NM_001354900.2:c.1156C>G