Canonical Allele Identifier: PA2827973369
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135729
ClinVar RCV Id: RCV000213708 RCV001192830 RCV001778740 RCV003650385 RCV003153407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser267Gly
CA015623
NM_001354899.2:c.799A>G