Canonical Allele Identifier: PA2573163436
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475817
ClinVar RCV Id: RCV002007963 RCV002423176 RCV003464343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu655Ser
CA346750588
NM_000179.3:c.1964T>C