Canonical Allele Identifier: PA915983947
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455553
ClinVar RCV Id: RCV000537127 RCV003372741 RCV004003744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn8Lys
CA346729470
NM_001258281.1:c.24T>A
CA346729471
NM_001258281.1:c.24T>G