Canonical Allele Identifier: PA645501798
Gene: CHRM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 228516
ClinVar RCV Id: RCV000222094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006631.1:p.Tyr18del
CA10576719
NM_001006630.2:c.52_54del