Canonical Allele Identifier: PA2825497237
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Asp1145Asn
CA5138155
NM_001083603.3:c.3433G>A