Canonical Allele Identifier: PA296590
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181213
ClinVar RCV Id: RCV000158586 RCV001850218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1042Asn
CA013364
NM_000257.4:c.3126G>T
CA389045452
NM_000257.4:c.3126G>C