Canonical Allele Identifier: PA131808
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42882
ClinVar RCV Id: RCV000035765 RCV000158509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly708Ala
CA011730
NM_000257.4:c.2123G>C