Canonical Allele Identifier: PA2828036670
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067905
ClinVar RCV Id: RCV002970748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341848.1:p.Asp151Tyr
CA374115021
NM_001354919.1:c.451G>T