Canonical Allele Identifier: PA2825510898
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2449648
ClinVar RCV Id: RCV003171667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Ile997Ser
CA374111657
NM_001083606.3:c.2990T>G