Canonical Allele Identifier: PA916071938
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180374
ClinVar RCV Id: RCV000157249 RCV003407587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Tyr50Ser
CA346369
NM_032714.3:c.149A>C