Canonical Allele Identifier: PA645489833
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312684
ClinVar RCV Id: RCV000393663 RCV002446566 RCV002480127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Thr376Ser
CA10639830
NM_022489.4:c.1126A>T
CA391215914
NM_022489.4:c.1127C>G