Canonical Allele Identifier: PA2826632516
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141232
ClinVar RCV Id: RCV000129648 RCV000459156 RCV000480608 RCV001354619 RCV003315879 RCV003997514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys707Ile
CA011400
NM_001281493.2:c.2120A>T