Canonical Allele Identifier: PA2825503899
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Ile957Val
CA16612665
NM_001083604.3:c.2869A>G