Canonical Allele Identifier: PA2825507846
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019544
ClinVar RCV Id: RCV001318990 RCV002456429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Met971Lys
CA196571104
NM_001083605.3:c.2912T>A