Allele Registry

Canonical Allele Identifier: PA132888

Gene: TNNT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000036624

RCV000148900

RCV000149450

RCV000588568

RCV000755701

RCV000771256

RCV000852592

RCV001081698

RCV001099310

RCV001099311

RCV002433498

ClinVar Variation:

43675

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000355.2:p.Ala38Val	CA004079 NM_000364.3:c.113C>T