Canonical Allele Identifier: PA2825507905
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448301
ClinVar RCV Id: RCV001997095 RCV002458871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Ile997Met
CA374111656
NM_001083605.3:c.2991T>G