Canonical Allele Identifier: PA2825350821
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052
ClinVar RCV Id: RCV000001107 RCV001380436 RCV003987303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg218Trp
CA114724
NM_001031714.3:c.652C>T