Canonical Allele Identifier: PA2825112197
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2847212
ClinVar RCV Id: RCV003750207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1068Tyr
CA389045211
NM_000257.4:c.3202G>T