Canonical Allele Identifier: PA658675649
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472862
ClinVar RCV Id: RCV000535958 RCV001112661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Pro1235Ser
CA7373370
NM_022489.4:c.3703C>T