Canonical Allele Identifier: PA645470994
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233385
ClinVar RCV Id: RCV000214711 RCV000812753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met26Leu
CA10577915
NM_000251.3:c.76A>C
CA346728665
NM_000251.3:c.76A>T