Canonical Allele Identifier: PA2828009618
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489476
ClinVar RCV Id: RCV000579432 RCV001800796 RCV003537232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp1919Ala
CA044147
NM_001354905.2:c.5756A>C