Canonical Allele Identifier: PA169553
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142842
ClinVar RCV Id: RCV000132280 RCV000800194 RCV000780435 RCV001753517 RCV003462042 RCV003998140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg39Pro
CA017407
NM_000251.3:c.116G>C