Canonical Allele Identifier: PA658744706
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489956
ClinVar RCV Id: RCV000580956 RCV000800340 RCV004001261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln349Glu
CA346741496
NM_000179.3:c.1045C>G