Canonical Allele Identifier: PA658804407
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 524957
ClinVar RCV Id: RCV000628875 RCV003162782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg281Lys
CA389051926
NM_000257.4:c.842G>A