Canonical Allele Identifier: PA915970303
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Leu984Pro
CA374111741
NM_001083607.3:c.2951T>C