Canonical Allele Identifier: PA2825351934
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439826
ClinVar RCV Id: RCV000507434 RCV000649999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Thr1011Arg
CA7373150
NM_001031714.3:c.3032C>G