Canonical Allele Identifier: PA645474370
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421295
ClinVar RCV Id: RCV000480852 RCV000775781 RCV001359758 RCV003470567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys491Asn
CA16617581
NM_000251.3:c.1473G>T
CA346727062
NM_000251.3:c.1473G>C