Canonical Allele Identifier: PA2825509331
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Thr274Met
CA337851
NM_001083606.3:c.821C>T