Canonical Allele Identifier: PA1139672332
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 966834
ClinVar RCV Id: RCV001241603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly464Ser
CA389050727
NM_000257.4:c.1390G>A