Canonical Allele Identifier: PA916071937
Gene: INF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 472837
ClinVar RCV Id: RCV000534855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116103.1:p.Tyr50Asp
CA391225100
NM_032714.3:c.148T>G