Canonical Allele Identifier: PA2828012708
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2586992
ClinVar RCV Id: RCV003341968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2397Ala
CA16037992
NM_001354905.2:c.7189T>G