Canonical Allele Identifier: PA2826464697
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 183758
ClinVar RCV Id: RCV000167995 RCV000162476 RCV000409730 RCV000480972 RCV000781560 RCV000708834 RCV004535054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp531Ala
CA019316
NM_001258281.1:c.1592A>C