Canonical Allele Identifier: PA2825497087
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 823625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Arg1112Cys
CA5138167
NM_001083603.3:c.3334C>T