Canonical Allele Identifier: PA658677584
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453850
ClinVar RCV Id: RCV000551653 RCV001020180 RCV003153669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Val1131Met
CA5138159
NM_000264.5:c.3391G>A