Canonical Allele Identifier: PA1139674583
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 920662
ClinVar RCV Id: RCV001179518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu707Asp
CA346750990
NM_000179.3:c.2121A>C
CA346750992
NM_000179.3:c.2121A>T