Canonical Allele Identifier: PA229135
Gene: ITSN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 100854
ClinVar RCV Id: RCV000087216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006268.2:p.Ala1578Ser
CA229134
NM_006277.3:c.4732G>T