Canonical Allele Identifier: PA645382181
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232501
ClinVar RCV Id: RCV000220336 RCV000691459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu818Phe
CA10578106
NM_000179.3:c.2452C>T