Canonical Allele Identifier: PA2825507870
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 835140
ClinVar RCV Id: RCV001035959 RCV003461430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Ser981Thr
CA374111760
NM_001083605.3:c.2941T>A