Canonical Allele Identifier: PA357500
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219619
ClinVar RCV Id: RCV000205023 RCV000565881 RCV000662459 RCV003997573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu312Val
CA041178
NM_000251.3:c.934C>G