Canonical Allele Identifier: PA658679970
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455351
ClinVar RCV Id: RCV000542898 RCV000567017 RCV003478110 RCV004003705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser28Leu
CA073484
NM_000179.3:c.83C>T