Canonical Allele Identifier: PA645474973
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237377
ClinVar RCV Id: RCV000228698 RCV000483596 RCV000575069 RCV003463648 RCV003998757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp646Ala
CA032095
NM_000251.3:c.1937A>C