Canonical Allele Identifier: PA645506422
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409153
ClinVar RCV Id: RCV000465324 RCV004022719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Ile1108Val
CA16612665
NM_000264.5:c.3322A>G