Canonical Allele Identifier: PA104372
Gene: SHH HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000184.1:p.Cys198Ser
CA370146721
NM_000193.4:c.593G>C
CA370146730
NM_000193.4:c.592T>A