Canonical Allele Identifier: PA645414981
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235026
ClinVar RCV Id: RCV000223878 RCV000818531 RCV002378957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg453Leu
CA10581177
NM_000257.4:c.1358G>T