Canonical Allele Identifier: PA2828036647
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 826296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341848.1:p.Ile144Val
CA374115067
NM_001354919.1:c.430A>G