Canonical Allele Identifier: PA196877
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187154
ClinVar RCV Id: RCV000166850 RCV000484988 RCV000629789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His1207Asp
CA013567
NM_000179.3:c.3619C>G