ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825490436
Gene: PTCH1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
646094
ClinVar RCV Id:
RCV000800312
RCV001815437
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001077071.1:p.Ser1066Phe
CA374111756
NM_001083602.3:c.3197C>T