Canonical Allele Identifier: PA2828034559
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Ile1096Thr
CA374111658
NM_001354918.1:c.3287T>C