Canonical Allele Identifier: PA2825486695
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1463621
ClinVar RCV Id: RCV001961144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.His318Pro
CA374119351
NM_001083602.3:c.953A>C