Canonical Allele Identifier: PA658671366
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483750
ClinVar RCV Id: RCV000574098 RCV000818613 RCV004001044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu12Gln
CA46666533
NM_000251.3:c.34G>C