Canonical Allele Identifier: PA915957491
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 639133
ClinVar RCV Id: RCV000791864 RCV001183376 RCV001759490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1645Arg
CA389037315
NM_000257.4:c.4935C>G
CA389037316
NM_000257.4:c.4935C>A
CA389037322
NM_000257.4:c.4933A>C