Canonical Allele Identifier: PA287456
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36578
ClinVar RCV Id: RCV000030254 RCV000212584 RCV000115531 RCV001079015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met141Val
CA021148
NM_000251.3:c.421A>G