Canonical Allele Identifier: PA658671483
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483666
ClinVar RCV Id: RCV000560975 RCV001867892 RCV003447542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala54Val
CA029814
NM_000251.3:c.161C>T