Canonical Allele Identifier: PA2828034443
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 941537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Glu1068Lys
CA374111837
NM_001354918.1:c.3202G>A