Canonical Allele Identifier: PA335730
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216347
ClinVar RCV Id: RCV000195508 RCV000581797 RCV001770148 RCV003114359 RCV003997016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met67Val
CA032335
NM_000251.3:c.199A>G