Canonical Allele Identifier: PA2828034420
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Arg1061His
CA348509
NM_001354918.1:c.3182G>A