Canonical Allele Identifier: PA162163
Gene: SMO HGNC NCBI

Linked Data

ClinVar Variation Id: 135258
ClinVar RCV Id: RCV000122072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005622.1:p.Ser33Arg
CA162162
NM_005631.5:c.99C>G
CA166249230
NM_005631.5:c.99C>A
CA369235017
NM_005631.5:c.97A>C