Canonical Allele Identifier: PA2827980918
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516
ClinVar RCV Id: RCV000034401 RCV000077995 RCV000130974 RCV000367966 RCV000987588 RCV001353889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2593Cys
CA014123
NM_001354899.2:c.7778C>G