Canonical Allele Identifier: PA2826465660
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90988
ClinVar RCV Id: RCV000115519 RCV000212621 RCV000410916 RCV000656882 RCV001082618 RCV003997162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn769His
CA020651
NM_001258281.1:c.2305A>C