Canonical Allele Identifier: PA2825507858
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730790
ClinVar RCV Id: RCV002451799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Leu976Val
CA374111788
NM_001083605.3:c.2926C>G