Canonical Allele Identifier: PA2580138087
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Leu968Val
CA374111841
NM_001083607.3:c.2902C>G