Canonical Allele Identifier: PA2825497172
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Val1130Met
CA5138159
NM_001083603.3:c.3388G>A