Canonical Allele Identifier: PA2827989996
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760927
ClinVar RCV Id: RCV002412240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2580Tyr
CA16038417
NM_001354900.2:c.7739C>A