Canonical Allele Identifier: PA2828009084
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630442
ClinVar RCV Id: RCV000775825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1821Thr
CA16034335
NM_001354905.2:c.5462A>C