Canonical Allele Identifier: PA2825351922
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 540041
ClinVar RCV Id: RCV000649963 RCV001811421 RCV002440353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026884.3:p.Asp997Asn
CA7373145
NM_001031714.3:c.2989G>A