Canonical Allele Identifier: PA2827973822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490192
ClinVar RCV Id: RCV000583252 RCV001192944 RCV003767276 RCV004001279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro413Thr
CA16024197
NM_001354899.2:c.1237C>A