Canonical Allele Identifier: PA2825351951
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447577
ClinVar RCV Id: RCV000518037 RCV002319517 RCV003766926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Thr1027Met
CA7373176
NM_001031714.3:c.3080C>T