Canonical Allele Identifier: PA2826635520
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023446
ClinVar RCV Id: RCV001323487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met352Ile
CA068329
NM_001281494.2:c.1056G>A
CA346750584
NM_001281494.2:c.1056G>C
CA346750585
NM_001281494.2:c.1056G>T