Canonical Allele Identifier: PA2825497211
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046910
ClinVar RCV Id: RCV001351531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Leu1137Val
CA374111726
NM_001083603.3:c.3409C>G