Canonical Allele Identifier: PA2827981338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482397
ClinVar RCV Id: RCV000573977 RCV003767148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2715Ser
CA050243
NM_001354899.2:c.8144A>G