Canonical Allele Identifier: PA164328
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41515
ClinVar RCV Id: RCV000034400 RCV000129389 RCV000200515 RCV003650357 RCV003996157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu2589Gly
CA014023
NM_001127510.3:c.7766A>G