Canonical Allele Identifier: PA2825499558
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 826366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Thr62Ala
CA374115047
NM_001083604.3:c.184A>G