Canonical Allele Identifier: PA645414486
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 380650
ClinVar RCV Id: RCV000435665 RCV000548210 RCV001524329 RCV002282140 RCV004022330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser4Leu
CA027806
NM_000257.4:c.11C>T