Canonical Allele Identifier: PA1139752154
Gene: INF2 HGNC NCBI
ClinVar RCV:
RCV001052524
ClinVar Variation:
848707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Gly63_Leu69del
CA916083401
NM_032714.3:c.188_208del