Canonical Allele Identifier: PA2826465017
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 584609
ClinVar RCV Id: RCV000708839 RCV001014077 RCV001064045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn605Ser
CA346729083
NM_001258281.1:c.1814A>G