Canonical Allele Identifier: PA2825513562
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Thr901Met
CA161680
NM_001083607.3:c.2702C>T