Canonical Allele Identifier: PA2825510814
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 947103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Asp959Asn
CA196571130
NM_001083606.3:c.2875G>A