Canonical Allele Identifier: PA658809642
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540039
ClinVar RCV Id: RCV000649961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071934.3:p.Arg1213Trp
CA7373328
NM_022489.4:c.3637C>T