Canonical Allele Identifier: PA645380550
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419196
ClinVar RCV Id: RCV000487153 RCV000582070 RCV000706852 RCV004002289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu546Gly
CA067957
NM_000179.3:c.1637A>G