Canonical Allele Identifier: PA2826465076
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408561
ClinVar RCV Id: RCV000468168 RCV001181992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val618Leu
CA16610822
NM_001258281.1:c.1852G>T
CA346729145
NM_001258281.1:c.1852G>C