Canonical Allele Identifier: PA2828036604
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714282
ClinVar RCV Id: RCV002297241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341848.1:p.His135Gln
CA374115123
NM_001354919.1:c.405T>A
CA374115124
NM_001354919.1:c.405T>G