Canonical Allele Identifier: PA645490241
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432619
ClinVar RCV Id: RCV000497978 RCV003766802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Ala1165Val
CA7373277
NM_022489.4:c.3494C>T