Canonical Allele Identifier: PA2825119759
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2845068
ClinVar RCV Id: RCV003608837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Met372Val
CA374119439
NM_000264.5:c.1114A>G