Canonical Allele Identifier: PA2826465134
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90881
ClinVar RCV Id: RCV000076383 RCV000501546 RCV000492029 RCV001034643 RCV003452886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro630Leu
CA019979
NM_001258281.1:c.1889C>T