Canonical Allele Identifier: PA195495
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186664
ClinVar RCV Id: RCV000166295 RCV000468110 RCV003227685 RCV003995498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met672Arg
CA019820
NM_000251.3:c.2015T>G