Canonical Allele Identifier: PA2825500624
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1760600
ClinVar RCV Id: RCV002409819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Gln266Leu
CA374118901
NM_001083604.3:c.797A>T