Canonical Allele Identifier: PA2828036641
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497340
ClinVar RCV Id: RCV003213795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341848.1:p.Glu142Gly
CA374115077
NM_001354919.1:c.425A>G