Canonical Allele Identifier: PA1139680765
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 923587
ClinVar RCV Id: RCV001184412 RCV003759014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser699Thr
CA346729225
NM_000251.3:c.2095T>A