Canonical Allele Identifier: PA2828034557
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428843
ClinVar RCV Id: RCV000492461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Phe1095Ser
CA374111664
NM_001354918.1:c.3284T>C