Canonical Allele Identifier: PA111367
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 30866
ClinVar RCV Id: RCV000023851 RCV001228020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Cys104Trp
CA129511
NM_022489.4:c.312C>G