Canonical Allele Identifier: PA916040590
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236617
ClinVar RCV Id: RCV000230741 RCV000586532 RCV000573026 RCV002487043 RCV003650530 RCV003998675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1779Thr
CA10582324
NM_001354896.2:c.5336A>C