Canonical Allele Identifier: PA2825508873
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067905
ClinVar RCV Id: RCV002970748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Asp66Tyr
CA374115021
NM_001083606.3:c.196G>T