Canonical Allele Identifier: PA2825119747
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788287
ClinVar RCV Id: RCV002428375 RCV003098744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Met363Thr
CA374119501
NM_000264.5:c.1088T>C