Canonical Allele Identifier: PA2827946632
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181815
ClinVar RCV Id: RCV000204441 RCV000216441 RCV000656749 RCV003998419 RCV003650407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.His2232Asp
CA012407
NM_001354895.2:c.6694C>G