Canonical Allele Identifier: PA2825503199
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 221968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Ile748Val
CA072669
NM_001083604.3:c.2242A>G