Canonical Allele Identifier: PA2825510899
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_001077075.1:p.Ile997Thr
CA374111658
NM_001083606.3:c.2990T>C