Canonical Allele Identifier: PA2828034560
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2449648
ClinVar RCV Id: RCV003171667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Ile1096Ser
CA374111657
NM_001354918.1:c.3287T>G