Canonical Allele Identifier: PA2825510825
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Arg962Cys
CA5138167
NM_001083606.3:c.2884C>T