Canonical Allele Identifier: PA132024
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43033
ClinVar RCV Id: RCV000035927 RCV003764667 RCV002336117 RCV003996213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1574Trp
CA015258
NM_000257.4:c.4720C>T