Canonical Allele Identifier: PA2825499507
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714282
ClinVar RCV Id: RCV002297241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.His50Gln
CA374115123
NM_001083604.3:c.150T>A
CA374115124
NM_001083604.3:c.150T>G