Canonical Allele Identifier: PA299329
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90782
ClinVar RCV Id: RCV000160595 RCV000212609 RCV000524360 RCV000662460 RCV000656879 RCV001357833 RCV003997153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met592Val
CA019271
NM_000251.3:c.1774A>G