Canonical Allele Identifier: PA2825492202
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1750238
ClinVar RCV Id: RCV002353505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Gln195Arg
CA374115164
NM_001083603.3:c.584A>G