Canonical Allele Identifier: PA2579923921
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587533
ClinVar RCV Id: RCV003360925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn903Lys
CA346731714
NM_000251.3:c.2709C>A
CA346731716
NM_000251.3:c.2709C>G