Canonical Allele Identifier: PA2825507834
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Val965Glu
CA338689
NM_001083605.3:c.2894T>A