Canonical Allele Identifier: PA2825505851
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453908
ClinVar RCV Id: RCV000526834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Cys52Tyr
CA374115112
NM_001083605.3:c.155G>A