Canonical Allele Identifier: PA2828031660
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453908
ClinVar RCV Id: RCV000526834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Cys203Tyr
CA374115112
NM_001354918.1:c.608G>A