Canonical Allele Identifier: PA2825505840
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 872551
ClinVar RCV Id: RCV001093088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Trp46Cys
CA374115153
NM_001083605.3:c.138G>T
CA374115154
NM_001083605.3:c.138G>C