Canonical Allele Identifier: PA2825489232
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.Met737Thr
CA374114313
NM_001083602.3:c.2210T>C