Canonical Allele Identifier: PA2573181319
Gene: ITGB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444107
ClinVar RCV Id: RCV001981652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120963.2:p.Arg393Ser
CA410485775
NM_001127491.3:c.1179G>T
CA410485776
NM_001127491.3:c.1179G>C