Canonical Allele Identifier: PA645490233
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 387417
ClinVar RCV Id: RCV000525037 RCV000757410 RCV001113918 RCV002323635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Gly1035Ser
CA7373180
NM_022489.4:c.3103G>A