Canonical Allele Identifier: PA2573164995
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374605
ClinVar RCV Id: RCV001883154 RCV002397817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu56Asp
CA346728984
NM_000251.3:c.168G>C
CA346728985
NM_000251.3:c.168G>T