ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825510901
Gene: PTCH1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
220370
ClinVar RCV Id:
RCV000206748
RCV000414011
RCV000575762
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001077075.1:p.Ile997Val
CA350753
NM_001083606.3:c.2989A>G