Canonical Allele Identifier: PA2825508872
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Met65Val
CA332595
NM_001083606.3:c.193A>G