Canonical Allele Identifier: PA2826463251
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246363
ClinVar RCV Id: RCV000236461 RCV001854870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys183Asn
CA10584209
NM_001258281.1:c.549G>C
CA346732305
NM_001258281.1:c.549G>T