Canonical Allele Identifier: PA2825503885
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Ala952Ser
CA374111934
NM_001083604.3:c.2854G>T