Canonical Allele Identifier: PA296905
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181392
ClinVar RCV Id: RCV000158868 RCV001181614 RCV001366342 RCV002492629 RCV003362701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1611Ser
CA015382
NM_000257.4:c.4831G>T