Canonical Allele Identifier: PA2826464635
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41645
ClinVar RCV Id: RCV000034553 RCV000115510 RCV000076263 RCV000148636 RCV000765667 RCV001079601 RCV001354468 RCV002265576 RCV003492329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn517Ser
CA019161
NM_001258281.1:c.1550A>G