Canonical Allele Identifier: PA645472565
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230221
ClinVar RCV Id: RCV000213764 RCV000506029 RCV000548278 RCV002243895 RCV003462428 RCV003997816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn285Lys
CA10577957
NM_000251.3:c.855C>G
CA346732846
NM_000251.3:c.855C>A