Canonical Allele Identifier: PA297892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181816
ClinVar RCV Id: RCV000159568 RCV000219951 RCV000409928 RCV001192797 RCV003315949 RCV003998420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2392Thr
CA012891
NM_001127510.3:c.7174C>A