Canonical Allele Identifier: PA2826465774
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455575
ClinVar RCV Id: RCV000547670 RCV001016009 RCV004003749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln795Leu
CA346731004
NM_001258281.1:c.2384A>T