Canonical Allele Identifier: PA132084
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43067
ClinVar RCV Id: RCV000035962 RCV000158697 RCV000471537 RCV000770470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1794Glu
CA016040
NM_000257.4:c.5380C>G