Canonical Allele Identifier: PA2579918890
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2673297
ClinVar RCV Id: RCV003455922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala604Asp
CA346728341
NM_000251.3:c.1811C>A