Canonical Allele Identifier: PA658738731
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489926
ClinVar RCV Id: RCV000579741 RCV000630172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro618Leu
CA346728438
NM_000251.3:c.1853C>T