Canonical Allele Identifier: PA296771
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806336
ClinVar RCV Id: RCV002470620 RCV003487037 RCV003994440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala199Thr
CA016506
NM_000257.4:c.595G>A