Canonical Allele Identifier: PA2825352104
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450497
ClinVar RCV Id: RCV000523280 RCV001857976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Asn1119Thr
CA7373231
NM_001031714.3:c.3356A>C