Canonical Allele Identifier: PA2825504026
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 237478

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Ser981Pro
CA10582674
NM_001083604.3:c.2941T>C