Canonical Allele Identifier: PA2826465825
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 935601
ClinVar RCV Id: RCV001204232 RCV003163542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys805Asn
CA346731125
NM_001258281.1:c.2415G>C
CA346731128
NM_001258281.1:c.2415G>T