Canonical Allele Identifier: PA2825351862
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796905
ClinVar RCV Id: RCV002435436 RCV003102794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Arg953Pro
CA391222789
NM_001031714.3:c.2858G>C