Canonical Allele Identifier: PA645379621
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428396
ClinVar RCV Id: RCV000491971 RCV001805109 RCV002523981 RCV004003461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp390Glu
CA067253
NM_000179.3:c.1170T>A
CA346742313
NM_000179.3:c.1170T>G