Canonical Allele Identifier: PA2828031701
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067905
ClinVar RCV Id: RCV002970748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Asp217Tyr
CA374115021
NM_001354918.1:c.649G>T