Canonical Allele Identifier: PA645457482
Gene: SHH HGNC NCBI

Linked Data

ClinVar Variation Id: 426566
ClinVar RCV Id: RCV000489667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000184.1:p.Arg28Ser
CA370152400
NM_000193.4:c.84G>T
CA370152403
NM_000193.4:c.84G>C