Canonical Allele Identifier: PA2825503911
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 947103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Asp959Asn
CA196571130
NM_001083604.3:c.2875G>A