Canonical Allele Identifier: PA645384523
Gene: SMO HGNC NCBI

Linked Data

ClinVar Variation Id: 245609
ClinVar RCV Id: RCV000236033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005622.1:p.Leu412Phe
CA10584652
NM_005631.5:c.1234C>T