Canonical Allele Identifier: PA916039967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188207
ClinVar RCV Id: RCV000168132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser924Ala
CA007751
NM_001354896.2:c.2770T>G