Canonical Allele Identifier: PA2827985052
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490261
ClinVar RCV Id: RCV000583866 RCV000611424 RCV002529141 RCV002491154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1081Ser
CA16028705
NM_001354900.2:c.3242A>G