Canonical Allele Identifier: PA2828034439
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Leu1067Val
CA374111841
NM_001354918.1:c.3199C>G