Canonical Allele Identifier: PA331384
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90791
ClinVar RCV Id: RCV000076292 RCV001854317 RCV002408595 RCV003460714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp603Gly
CA019354
NM_000251.3:c.1808A>G