Canonical Allele Identifier: PA658736520
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 495772
ClinVar RCV Id: RCV000590002 RCV001024159 RCV001853977 RCV004002418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln183Lys
CA346730870
NM_000251.3:c.547C>A