Canonical Allele Identifier: PA2825507838
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098194
ClinVar RCV Id: RCV003019135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Ala967Ser
CA5138164
NM_001083605.3:c.2899G>T