Canonical Allele Identifier: PA2825497241
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Ile1147Thr
CA374111658
NM_001083603.3:c.3440T>C