Canonical Allele Identifier: PA645489819
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 388001
ClinVar RCV Id: RCV000428001 RCV001221125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Arg261Gln
CA7372422
NM_022489.4:c.782G>A