Canonical Allele Identifier: PA174032
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 132908
ClinVar RCV Id: RCV000148955 RCV001781460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp896Asn
CA012857
NM_000257.4:c.2686G>A