Canonical Allele Identifier: PA2826464754
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1400256
ClinVar RCV Id: RCV001918100 RCV003365531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe542Leu
CA346728356
NM_001258281.1:c.1624T>C
CA346728361
NM_001258281.1:c.1626T>G
CA346728362
NM_001258281.1:c.1626T>A