Canonical Allele Identifier: PA2825500517
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Ala242Thr
CA254347
NM_001083604.3:c.724G>A