Canonical Allele Identifier: PA2826463829
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232371
ClinVar RCV Id: RCV000214618 RCV000480571 RCV000409794 RCV000761006 RCV000546544 RCV003387810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg316Cys
CA027079
NM_001258281.1:c.946C>T