Canonical Allele Identifier: PA2825492282
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497340
ClinVar RCV Id: RCV003213795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Glu207Gly
CA374115077
NM_001083603.3:c.620A>G