Canonical Allele Identifier: PA915970284
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Val975Ile
CA161694
NM_001083607.3:c.2923G>A