Canonical Allele Identifier: PA2827981036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761367
ClinVar RCV Id: RCV002416871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2624Tyr
CA16038605
NM_001354899.2:c.7871C>A