Canonical Allele Identifier: PA2827992857
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611
ClinVar RCV Id: RCV000480278 RCV000580908 RCV002526522 RCV004002260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Tyr678His
CA031174
NM_001354901.2:c.2032T>C