Canonical Allele Identifier: PA2499230080
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008707
ClinVar RCV Id: RCV001306086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys659Asn
CA346728853
NM_000251.3:c.1977A>C
CA346728854
NM_000251.3:c.1977A>T