Canonical Allele Identifier: PA2827978022
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587019
ClinVar RCV Id: RCV003341980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1709Asn
CA16032719
NM_001354899.2:c.5126G>A