Canonical Allele Identifier: PA916021151
Gene: SHH HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001297391.1:p.Trp30Arg
CA340832
NM_001310462.2:c.88T>C
CA370149349
NM_001310462.2:c.88T>A