Canonical Allele Identifier: PA658672761
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485839
ClinVar RCV Id: RCV000564234 RCV000629939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val617Leu
CA346728421
NM_000251.3:c.1849G>C