Canonical Allele Identifier: PA645470939
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245828
ClinVar RCV Id: RCV000235367 RCV000572196 RCV000688689 RCV003463696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser13Asn
CA10584201
NM_000251.3:c.38G>A