Allele Registry

Canonical Allele Identifier: PA104495

Gene: SHH HGNC NCBI

ClinVar RCV:

RCV000009427

ClinVar Variation:

8877

HGVS (amino-acid)	Matching Registered Transcripts
NP_000184.1:p.Gly31Arg	CA340826 NM_000193.4:c.91G>A CA370152346 NM_000193.4:c.91G>C