Canonical Allele Identifier: PA2825499524
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Lys54Thr
CA374115098
NM_001083604.3:c.161A>C