Canonical Allele Identifier: PA2827940872
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193
ClinVar RCV Id: RCV000582096 RCV003653189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala449Val
CA16024253
NM_001354895.2:c.1346C>T