Canonical Allele Identifier: PA296571
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181203
ClinVar RCV Id: RCV000158568 RCV000628883 RCV000769454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Cys905Ser
CA012920
NM_000257.4:c.2714G>C
CA389047304
NM_000257.4:c.2713T>A