Canonical Allele Identifier: PA645382650
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410472
ClinVar RCV Id: RCV002230116 RCV004022785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro903Leu
CA16610917
NM_000179.3:c.2708C>T