Canonical Allele Identifier: PA915984042
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 619868
ClinVar RCV Id: RCV000759831 RCV001855919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys47Asn
CA346730036
NM_001258281.1:c.141G>T
CA346730037
NM_001258281.1:c.141G>C