Canonical Allele Identifier: PA2828031677
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497340
ClinVar RCV Id: RCV003213795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Glu208Gly
CA374115077
NM_001354918.1:c.623A>G