Canonical Allele Identifier: PA645384333
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421923
ClinVar RCV Id: RCV000480946 RCV001048449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His1207Gln
CA071509
NM_000179.3:c.3621T>G
CA346760587
NM_000179.3:c.3621T>A