Canonical Allele Identifier: PA915970151
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 826296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Ile59Val
CA374115067
NM_001083607.3:c.175A>G