Canonical Allele Identifier: PA2825351069
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429808
ClinVar RCV Id: RCV000493332 RCV001205939 RCV003380593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Val383Met
CA7372519
NM_001031714.3:c.1147G>A