Canonical Allele Identifier: PA2825507814
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Ile957Val
CA16612665
NM_001083605.3:c.2869A>G