Canonical Allele Identifier: PA2828034433
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2006893
ClinVar RCV Id: RCV002837976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Leu1065Val
CA374111852
NM_001354918.1:c.3193C>G