Canonical Allele Identifier: PA2826464277
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246481
ClinVar RCV Id: RCV000236460 RCV001047851 RCV003165662 RCV003998929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met426Leu
CA028758
NM_001258281.1:c.1276A>T
CA346727068
NM_001258281.1:c.1276A>C