Canonical Allele Identifier: PA2825119180
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753216
ClinVar RCV Id: RCV002354092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Thr213Arg
CA374115044
NM_000264.5:c.638C>G