Canonical Allele Identifier: PA2827956949
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_001341826.1:p.Ser916Ala
CA007751
NM_001354897.2:c.2746T>G