Canonical Allele Identifier: PA2825111517
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1792571
ClinVar RCV Id: RCV002433075 RCV003748443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys841Asn
CA389048235
NM_000257.4:c.2523G>T
CA389048236
NM_000257.4:c.2523G>C