Canonical Allele Identifier: PA346370
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_071934.3:p.Tyr50Ser
CA346369
NM_022489.4:c.149A>C