Canonical Allele Identifier: PA2825509310
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760600
ClinVar RCV Id: RCV002409819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Gln266Leu
CA374118901
NM_001083606.3:c.797A>T