Canonical Allele Identifier: PA2826463506
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502458
ClinVar RCV Id: RCV002010990 RCV003585188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu244Phe
CA346732997
NM_001258281.1:c.730C>T