Canonical Allele Identifier: PA338109
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216343
ClinVar RCV Id: RCV000986673 RCV001201365 RCV000774569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser516Asn
CA338107
NM_000251.3:c.1547G>A