Canonical Allele Identifier: PA2499230083
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171156
ClinVar RCV Id: RCV001524078 RCV001872015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile685Leu
CA346729149
NM_000251.3:c.2053A>C
CA346729150
NM_000251.3:c.2053A>T