Canonical Allele Identifier: PA2579923846
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230841
ClinVar RCV Id: RCV004522955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met899Leu
CA346731604
NM_000251.3:c.2695A>T
CA346731610
NM_000251.3:c.2695A>C