Canonical Allele Identifier: PA2828046489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 644645
ClinVar RCV Id: RCV001025757 RCV003535900 RCV003318638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2169Ala
CA16036352
NM_001354904.2:c.6505T>G