Canonical Allele Identifier: PA658672563
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479787
ClinVar RCV Id: RCV000567489 RCV000662462 RCV001039308 RCV003153734 RCV004000846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg534Leu
CA029754
NM_000251.3:c.1601G>T