Canonical Allele Identifier: PA2826464778
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41647
ClinVar RCV Id: RCV000034555 RCV000705544 RCV000771463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn547His
CA019422
NM_001258281.1:c.1639A>C