Canonical Allele Identifier: PA2828034558
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220370
ClinVar RCV Id: RCV000206748 RCV000414011 RCV000575762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Ile1096Val
CA350753
NM_001354918.1:c.3286A>G