Canonical Allele Identifier: PA16040006
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998
ClinVar RCV Id: RCV000217497 RCV002515686 RCV003477752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1697Ala
CA10578392
NM_000038.6:c.5089A>G