Canonical Allele Identifier: PA2828034436
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098194
ClinVar RCV Id: RCV003019135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Ala1066Ser
CA5138164
NM_001354918.1:c.3196G>T