ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828034559
Gene: PTCH1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1040725
ClinVar RCV Id:
RCV001344416
RCV002456491
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341847.1:p.Ile1096Thr
CA374111658
NM_001354918.1:c.3287T>C