Canonical Allele Identifier: PA2825496953
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Val1082Met
CA215710
NM_001083603.3:c.3244G>A