Canonical Allele Identifier: PA2826465285
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216350
ClinVar RCV Id: RCV000236347 RCV000491392 RCV000524380 RCV000656998 RCV000662875 RCV001358322 RCV003153472 RCV004530190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala667Thr
CA034588
NM_001258281.1:c.1999G>A