Canonical Allele Identifier: PA645476333
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230103
ClinVar RCV Id: RCV000220752 RCV003758729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn903Ser
CA10578015
NM_000251.3:c.2708A>G