Canonical Allele Identifier: PA131991
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43009
ClinVar RCV Id: RCV000995146 RCV001170993 RCV001241747 RCV001841564 RCV002326730 RCV004017302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1450Asn
CA014834
NM_000257.4:c.4348G>A