Canonical Allele Identifier: PA658673068
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455565
ClinVar RCV Id: RCV000550167 RCV000567964 RCV003459179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn835Ser
CA036330
NM_000251.3:c.2504A>G