Canonical Allele Identifier: PA2825282035
Gene: CHRM2 HGNC NCBI
ClinVar RCV:
RCV000222094
ClinVar Variation:
228516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006632.1:p.Tyr18del
CA10576719
NM_001006631.3:c.52_54del