Canonical Allele Identifier: PA2826626684
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410510
ClinVar RCV Id: RCV000461074 RCV001013909 RCV003320187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met532Val
CA16610994
NM_001281492.2:c.1594A>G