Canonical Allele Identifier: PA645490232
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312704
ClinVar RCV Id: RCV000269885 RCV000691072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Thr996Ile
CA7373144
NM_022489.4:c.2987C>T