Canonical Allele Identifier: PA2828017120
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_001341832.1:p.Tyr636His
CA031174
NM_001354903.2:c.1906T>C