Canonical Allele Identifier: PA2825021428
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1524741
ClinVar RCV Id: RCV003773518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1718Ser
CA16032593
NM_000038.6:c.5152G>T