ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826990174
Gene: INVS
HGNC
NCBI
Linked Data
ClinVar Variation Id:
289200
ClinVar RCV Id:
RCV000310454
RCV001859698
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305310.1:p.Leu849His
CA5158723
NM_001318381.2:c.2546T>A