ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825511000
Gene: PTCH1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000121893
RCV000127647
RCV000266478
RCV000361116
RCV000492383
ClinVar Variation:
135100
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001077075.1:p.Thr1044Ser
CA161704
NM_001083606.3:c.3130A>T